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Malherbe et al. Rare Dis Orphan Drugs J 2024;3:7  https://dx.doi.org/10.20517/rdodj.2023.49  Page 5 of 11



 Table 1. Summary of biochemical NBS results, Centre for Metabolomics, North-West University, January 1998-September 2023. All 125,888 samples (equivalent to 0.5% of births in South
 Africa) were screened using a panel of 22 conditions

 year  Project  Total samples  Total positive  PA  MMA IVA GAI BIOT PKU GALT CH CAH CF 3-MCC  TYRI TFP/LCHAD  CUD OTC MADD/GAII
 RUSP core conditions                                                   Secondary conditions
 1998  Government   445  0

 1999  Government   4,903  0
 2000  Government   8,410  1  1
 2001  Government   10,674  1  1
 2002  Government   8,886  0

 2003  Government   11,399  1  1
 2004  Government   12,665  1  1
 2005  Government   11,933  0
 2006  Government   3,121  0
 2007  Private   106  0

 2008  Private   1,325  0
 2009  Private   1,163  3  1  2
 2010  Private  871  3  1  1  1
 2011  Private   811  0

 2012  Private   951  5  1  1  1  1  1
 2013  Private   1,770  1  1
 2014  Private   2,897  9  1  1 + 1*  1  1  3                                  1
 2015  Private   3,442  6  1  1  1  2  1
 2016  Private   4,245  1  1

 2017  Private   5,486  1  1
 2018  Private   5,596  8  4  2  1  1
 2019  Private   5,567  5  3              1                             1
 2020  Private   5,346  11  3  1  3  1  1  1  1

 2021  Private   5,362  13  2 + 3*  1  2  1      1               2      1
 2022  Private   4,702  5  1  2  1                                      1
 2023  Private   3,812  5  3  1  1
 Total  125,888  80  10  2  3  2  14  3  10  16  4  6  2  1  1   2      3      1


 *Indicates cases unconfirmed via further review following initial positive screening. PA: Propionic acidaemia; MMA: methylmalonic acidaemia; IVA: isovaleric acidaemia; GAI: glutaric acidaemia type I; BIOT:
 biotinidase deficiency; PKU: phenylketonuria; GALT: galactosaemia due to GALT deficiency; CH: (primary) congenital hypothyroidism; CAH: congenital adrenal hyperplasia; CF: cystic fibrosis; 3-MCC: 3-
 methylcrotonyl-CoA carboxylase deficiency;   TYRI: tyrosinemia type I;   TFP/LCHAD: trifunctional  protein deficiency/long-chain hydroxyacyl-CoA dehydrogenase deficiency;   CUD: carnitine uptake disorder;  OTC:
 ornithine transcarbamylase deficiency; MADD/GAII: multiple acyl-CoA dehydrogenase deficiency/glutaric acidaemia type 2. A RUSP “secondary condition” is identified unintentionally when screening for one of the
 core conditions; or as a consequence of confirmatory testing for an out-of-range result of a core condition.
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